Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,614 in last 12 months

Showing 1232112340 of 28,172 recalls

Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Zimmer Surgical Inc

Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...

The Issue: When inflating/deflating a single bladder, both bladders could potentially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Ethicon, Inc.

Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...

The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· Clinical Diagnostic Solutions, Inc.

Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...

The Issue: A mix-up of autosampler tube positions with a possibility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing